# Feeder-Free Expanded and Cryopreserved NK Cells Retain Antibody-Dependent Cell Cytotoxicity against HER2-Positive Tumors

**Authors:** Injee Lee, Suwoo Kim, Chaeyeon Jin, KyuBum Kwack, Youngseok Baek

PMC · DOI: 10.4014/jmb.2507.07016 · Journal of Microbiology and Biotechnology · 2025-10-29

## TL;DR

Researchers developed a method to expand and freeze NK cells that retain their ability to kill HER2-positive tumors when combined with trastuzumab.

## Contribution

A feeder-free expansion and cryopreservation method for NK cells that preserves their ADCC activity against HER2-positive tumors.

## Key findings

- Feeder-free expansion increased CD16 expression and enhanced ADCC activity in NK cells.
- Cryopreserved NK cells maintained antitumor efficacy comparable to freshly expanded cells.
- The method supports scalable and safe NK cell therapies for both allogeneic and autologous use.

## Abstract

CAR-T, TIL, and TCR-based T cell immunotherapies have revolutionized cancer treatment; however, their clinical application remains limited by severe adverse effects such as CRS, ICANS, and HLH, as well as the risk of GvHD in the allogeneic setting. In contrast, NK cell-based therapies have emerged as a safer alternative with minimal adverse effects and can be developed from diverse cellular sources. Nevertheless, clinical translation of NK cell therapies is challenged by difficulties in large-scale expansion, donor variability, and high sensitivity to cryopreservation. In this study, we established a feeder-free culture system that selectively activated and expanded NK cells directly from peripheral blood mononuclear cells (PBMCs) without prior depletion of T or B cells. The expanded NK cells exhibited increased CD16 expression compared with naïve NK cells and demonstrated enhanced antitumor activity through antibody-dependent cellular cytotoxicity (ADCC) when combined with trastuzumab. To overcome limitations in long-term storage, NK cells were cryopreserved using a formulation containing 5% dimethyl sulfoxide (DMSO) supplemented with sugars and albumin. Importantly, the in vivo antitumor efficacy of cryopreserved NK cells was found to be comparable to that of freshly expanded NK cells. These findings show that feeder-free expanded NK cells possess potent ADCC activity and that optimized cryopreservation strategies can preserve therapeutic efficacy, supporting their clinical applicability and scalability as not only off-the-shelf allogeneic products but also personalized autologous NK cell therapies.

## Linked entities

- **Proteins:** FCGR3B (Fc gamma receptor IIIb)
- **Chemicals:** dimethyl sulfoxide (PubChem CID 679), DMSO (PubChem CID 679)
- **Diseases:** cancer (MONDO:0004992), HLH (MONDO:0015540), CRS (MONDO:0007399), GvHD (MONDO:0013730)

## Full-text entities

- **Genes:** FCGR3A (Fc gamma receptor IIIa) [NCBI Gene 2214] {aka CD16-II, CD16A, FCG3, FCGR3, FCRIIIA, FcGRIIIA}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** CRS (MESH:D003398), Tumors (MESH:D009369), GvHD (MESH:D006086)
- **Chemicals:** DMSO (MESH:D004121), sugars (MESH:D000073893), trastuzumab (MESH:D000068878)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12603374/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12603374/full.md

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Source: https://tomesphere.com/paper/PMC12603374